Device recall
Z-1520-06: OASIS Medical SOFT PLUG Extended Duration Plug, Reference 6403 (Lot LA1105E)
FDA device recall · Class III · Oasis Medical Inc
Key facts
| Recall number (Z-number) | Z-1520-06 |
|---|---|
| Recall event | 36277 |
| Product | OASIS Medical SOFT PLUG Extended Duration Plug, Reference 6403 (Lot LA1105E) |
| Product code | LZU |
| Recalling firm | Oasis Medical Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 1, 2011 |
| 510(k) numbers | K013613 |
| FEI number | 2083373 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database